(EU) 2017/745 Medical Device Regulation Certification

The CE marking indicates that the products comply with the provisions set out in the technical regulations of the EU and can be released into free circulation within the EU without. SZUTEST Konformitätsbewertungsstelle GmbH is recognized by the Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (ZLG) and EU Commission, as a Notified Body with the identification number 2975 under the Medical Device Regulation (EU) 2017/745.